HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717596Generated: October 31, 2026
3,4-Difluoro-2-(2-fluoro-4-iodoanilino)benzoyl fluoride → HCID 59469195, compound
https://huagongshe.com/reaction/1717596
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4-Difluoro-2-(2-fluoro-4-iodoanilino)benzoyl fluoride | HCID 59469158 | — |
| Reactant | HCID 67051825 | HCID 67051825 | — |
| Product | HCID 59469195 | HCID 59469195 | — |
Reaction Steps
The compounds of examples 25a and 25b were synthesized starting from benzyl 3-hydroxy-3-(2-oxycyclohenyl)azetidine-1-carboxylate prepared according to the procedure given in example 25. The ketone was reduced to give benzyl 3-hydroxy-3-(2-hydroxycyclohexyl)azetidine-1-carboxylate as a mixture of racemic diastereomers which were subjected to hydrogenation to afford 3-(2-hydroxycyclohexyl)azetidin-3-ol. 3-(2-hydroxycyclohexyl)azetidin-3-ol was then carried forward in a coupling step with 3,4-difluoro-2-(2-fluoro-4-iodophenylamino)benzoyl fluoride in the usual manner. The coupled material thus obtained was purified by preparative reverse phase HPLC where fraction 1 was tentatively assigned as (±)-1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)-3-[(trans)-2-hydroxycyclohexyl]azetidin-3-ol (Example 25a) and fraction 2 was tentatively assigned as (±)-1-({3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]phenyl}carbonyl)-3-[(cis)-2-hydroxycyclohexyl]azetidin-3-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07803839B2 |
|---|
| Source dataset | uspto-grants-2010_09 |
|---|
| ORD ID | ord-254e33cd96694d86b9146e334d762bb8 |
|---|
| Source note | uspto-grants-2010_09 |
|---|